A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632004



Internal ID7018814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47262090..47266505hg38UCSC Ensembl
Innerchr13:47262090..47266505hg38UCSC Ensembl
Outerchr13:47261965..47266661hg38UCSC Ensembl
chr13:47836225..47840640hg19UCSC Ensembl
Innerchr13:47836225..47840640hg19UCSC Ensembl
Outerchr13:47836100..47840796hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg384416
hg194416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14713649
SamplesNA18963
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632004
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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